448 English-speaking jobs in Walloon Brabant

Validation Engineer will lead and execute process and equipment validation activities for pharmaceutical products. Responsibilities include developing validation master plans, conducting risk assessments, and ensuring compliance with EU GMP, ICH guidelines, and Belgian regulations.

The Global Study Manager is responsible for delivering clinical study operations from study initiation to archiving. This role involves developing and executing study plans, managing vendors, ensuring compliance with regulations, and leading study teams to achieve objectives. The GSM collaborates with the Global Study Lead and leads the Operational Working Group. Requires a Bachelor's degree in a life science field, 5+ years of study management experience, and in-depth knowledge of GCPs and ICH guidelines.

Leads global sales vision and strategy for IBA's Industrial Business Unit. Manages a team of 10 sales professionals across Asia, US, and Europe. Develops and executes sales plans to achieve business growth objectives. Requires 15+ years of international sales experience in industrial solutions or related sectors.

Develop and validate robust analytical methods using modern statistical approaches. Collaborate with cross-functional teams to ensure successful method transfer and lifecycle management. Document results and communicate findings to stakeholders.

Leads asset-level clinical operations planning, ensuring inspection readiness and regulatory deliverables. Contributes to the Clinical Development Plan and Integrated Evidence Plan. Represents Global Clinical Operations functions at the asset level. Coordinates cross-functional partners to support timely data deliveries. Oversees vendor selection, contracting, and operational oversight for outsourced clinical activities. Provides strategic guidance to Study Delivery Teams. Prepares and responds to data requests and contributes to regulatory submission materials.

Principal Technician to design, implement, and maintain core network architecture for large organizations. Requires a Bachelor's degree and 2 years of experience or 6 years of relevant experience. Must have experience with network hardware/software, ITIL principles, and public cloud technologies.

Accountant will process customer invoices, manage intercompany operations, and reconcile AR accounts. Experience in a similar role (1-2 years) is required.

Freelance Senior Business Analyst specializing in Odoo solutions needed for ERP implementation projects. Must have experience in functional analysis, business process modeling, and Odoo module configuration. Fluent in French and English.

This 6-month contract role is responsible for preparing, facilitating, and following up on Quality councils. The Specialist will drive inspection readiness, define and coordinate QA oversight and inspections, and follow up on complaint investigations. They will also ensure QMS alignment and manage quality escalations.

Lead quality processes for digital clinical devices, from concept to deployment, ensuring regulatory compliance and innovation velocity. Design quality frameworks, prioritize activities based on risk, and translate technical requirements into actionable guidance. Collaborate with cross-functional teams, communicate quality concepts to diverse audiences, and propose innovative solutions.

Leads global quality team, drives continuous improvement initiatives, and ensures performance excellence across internal manufacturing sites. Collaborates with stakeholders to harmonize processes, optimize operations, and implement digitalization strategies. Manages KPIs, supports audits, and fosters a culture of innovation. Requires a Bachelor's or Master's degree in a relevant scientific discipline and 10+ years of experience in Quality Assurance, Quality Systems Operations, or Quality Compliance within a regulated pharmaceutical environment. Fluent English required.

Leads a global quality team, oversees Qualification and Validation activities, and ensures compliance with global Data Integrity standards. Collaborates with internal and external manufacturing organizations to harmonize quality practices and drive continuous improvement. Requires a Bachelor's or Master's degree in a relevant scientific discipline and 10+ years of experience in Quality Assurance, Quality Systems Operations, or Quality Compliance within a regulated pharmaceutical environment.

Application Developer to support mission-critical business applications within the Oracle ecosystem. Responsibilities include providing 2nd and 3rd line support, contributing to analysis, design, and implementation of new requirements, and ensuring full lifecycle testing.

Site-based Health Safety Environment Advisor responsible for driving health, safety, and environmental standards across a project.

Site-based Health Safety Environment Advisor responsible for driving health, safety, and environmental standards across a project.

VeraSafe seeks an IT Security Advisor to join its growing cybersecurity consulting team. The role involves managing client relationships, conducting cybersecurity risk assessments, and providing fractional CISO-type support. Responsibilities include developing and delivering security assessments, implementing security controls, and collaborating with clients to meet their IT security needs.

VeraSafe seeks an IT Security Advisor to join its growing cybersecurity consulting team. The role involves managing client relationships, conducting cybersecurity risk assessments, and providing fractional CISO-type support. Responsibilities include developing and delivering security assessments, implementing security controls, and collaborating with clients to meet their IT security needs.

Leads sales and strategy for medical imaging hardware and AI-based pathology software across India, Australia/New Zealand, Southeast Asia, and South Korea. Manages global accounts, develops regional growth strategies, and collaborates with marketing and clinical teams.

Leads sales and strategy for medical imaging hardware and AI-based pathology software across India, Australia/New Zealand, Southeast Asia, and South Korea. Manages global accounts, develops regional growth strategies, and collaborates with marketing and clinical teams.

Develops and defines technical standards for Sterile Drug Product and Dry Forms Drug Product Equipment Design. Monitors technological developments and leads a global network of experts to ensure best practices. Assists in technical and peer review of projects, ensuring adherence to cGMPs, SOPs, and Good Engineering Practices.